Skip to main content

Advertisement

Log in

Effect of starving and feeding on some haematological and physiological responses of the Nile catfish, Clarias gariepinus exposed to copper at extreme seasons

  • Published:
Fish Physiology and Biochemistry Aims and scope Submit manuscript

Abstract

The lethal concentration for 50% of fish for 96h (96h LC50) of copper (Cu2+) was estimated for the Nile catfish (Clarias gariepinus) in extreme seasons, winter and summer, 4.31 and 4.79 mg/l, respectively. The Nile catfish was exposed to 96h LC50 of copper for 7 days in extreme winter and summer. The body indices, haematological parameters as well as some plasma and liver enzyme activities and metabolite level were significantly differed in fish exposed to copper over than those of the control fish. Most of the tested parameters were not significantly different between the control fish of winter and summer (winter, water temperature 18 ± 2°C and summer, 27 ± 2°C). The effect of two ration sizes on copper toxicity in two different seasons on C. gariepinus was justified. It was found that the haematological parameters and the tested plasma activities of enzymes were significantly valid due to season differences. The blood parameters as well as plasma activities of enzymes were significantly differed in fishes fed elevated ration (3%) and exposed to copper challenge. On the other hand, the exploit of low feeding ration (0.5%) along with copper exposure during the examined seasons induced non-significant differences of the tested parameters, from those of the corresponding control. Therefore, the low feeding ration provides some tolerance against the possible water-borne copper exposure.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Subscribe and save

Springer+
from $39.99 /Month
  • Starting from 10 chapters or articles per month
  • Access and download chapters and articles from more than 300k books and 2,500 journals
  • Cancel anytime
View plans

Buy Now

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  • Abdel-Hameid NAH (2007) Physiological and histological changes induced by phenol exposure in Oreochromis aureus juveniles. Turk J Fish Aquat Sci 7:131–138

    Google Scholar 

  • Abdel-Tawwab M, Mousa MAA, Ahmad MH, Sakr SF (2007) The use of calcium pre-exposure as a protective agent against environmental copper toxicity for juvenile Nile tilapia, Oreochromis niloticus (L.). Aquaculture 264:236–246

    Article  CAS  Google Scholar 

  • Ahmad I, Oliveria M, Pachcco M, Santos MA (2005) Anguilla anguilla L. oxidative stress biomarkers responses to copper exposure with or without β-naphthoflavone pre-exposure. Chemosphere 61:267–275

    Article  PubMed  CAS  Google Scholar 

  • Ahmed MH, El-Marakby HI, Seden MEA, Abdel-Tawwab M, Abou-El-Atta ME (2006) The use of organic selenium (Sel-PlexO) in practical diets of Nile tilapia, Oreochromis niloticus (L.): effect on growth performance, feed utilization, whole body composition and entropathogeic Aeromonas hydrophila-challenge. In: Contreas W, Fitzsimmons K (eds) 7th international symposium on Tilapia in aquaculture. Boca del Rio, Veracruz, Mexico, 6–8 Sept 2006, pp 95–107

  • Ahmed I, Maria VI, Oliveria M, Pacheco M, Santos MA (2007) European eel (Anguilla anguilla) gill and kidney genotoxic response to copper exposure with or without β-naphthoflavone pre-exposure. Third biennial meeting of the Society for Free Radical Research-Asia (SFR-Asia) and sixth annual meeting of the Society for free Radical Research-India (SFRR-India), Jan 8–11 2007, Lonavalva, India, p 96

  • Ali M, Nicieza A, Wooton RJ (2003) Compensatory growth in fishes: a response to growth depression. Fish Fisher 4:147–190

    Article  Google Scholar 

  • An Y, Kampbell DH (2003) Total, dissolved, and bioavailable metals at Lake Texoma marinas. Environ Pollut 122(2):253–259

    Google Scholar 

  • Bagnykova TV, Lushchak OV, Storey KB, Lushchak VI (2007a) Oxidative stress and antioxidant defense responses by goldfish tissues to acute change of temperature from 3°C to 23°C. J Therm Biol 32:227–234

    Article  Google Scholar 

  • Bagnykova TV, Danyliv SI, Zin’ko OS, Lushchak VI (2007b) Heat shock induces oxidative stress in rotan Perccottus glenii tissues. J Therm Biol 32:225–260

    Google Scholar 

  • Barse AV, Chakrabarti T, Ghosh TK, Pal AK, Jadhao SB (2006) One-tenth dose of LC50 of 4-tert-butylphenol causes endocrine disruption and metabolic changes in Cyprinus carpio. Pest Biochem Physiol 86(3):172–179

    Article  CAS  Google Scholar 

  • Beaumont MW, Taylor EW, Butler PJ (2000) The resting membrane potential of white muscle from brown trout (Salmo trutta) exposed to cooper in soft, acidic water. J Exp Biol 203:2229–2236

    PubMed  CAS  Google Scholar 

  • Beaumont MW, Butler PJ, Taylor FW (2003) Exposure of brown trout Salmo trutta to a sublethal concentration of copper in soft acidic water: effects upon gas exchange and ammonia accumulation. J Exp Biol 206:153–162

    Article  PubMed  CAS  Google Scholar 

  • Begum G, Vijayaraghavan S (1995) Carbohydrate metabolism in hepatic tissue of fresh water Clarias batrachus L. during dimethoate exposure. Fd Chem Toxic 33:423–426

    Article  CAS  Google Scholar 

  • Bernet D, Schmidt H, Wahli T, Burkhardt-Holm P (2001) Effluent from a sewage treatment works causes changes in serum biochemistry of brown trout (Salmo trutta L.). Ecotoxicol Environ Saf 48:140–147

    Article  PubMed  CAS  Google Scholar 

  • Blaxhall PC, Daisely KW (1973) Routine hematological methods for use with fish blood. J Fish Biol 5:681–771

    Google Scholar 

  • Carriquiriborde P, Handy RD, Davies SJ (2004) Physiological modulation of iron metabolism in rainbow trout (Oncorhynchus mykiss) fed low and high iron diets. J Exp Biol 207:75–86

    Article  PubMed  CAS  Google Scholar 

  • Carvalho CS, Fernandes MN (2006) Effect of temperature on copper toxicity and hematological responses in the neotropical fish Prochilodus scrofa at low and high pH. Aquaculture 251:109–117

    Article  CAS  Google Scholar 

  • Carvalho CS, Fernandes MN (2008) Effect of copper on liver key enzymes of anaerobic glucose metabolism from freshwater tropical fish Prochilodus lineatus. Comp Biochem Physiol A 151(3):437–442

    Article  Google Scholar 

  • Cnaani A, Tinman S, Avidar RonM, Hulata G (2004) Comparative study of biochemical parameters in response to stress in Oreochromis aureu. O. mossambicus and two strains of O. niloticus. Aquac Res 35:1434–1440

    Article  CAS  Google Scholar 

  • Dacie JV, Lewis SN (1984) Practical haematology, 5th edn. J & Churchill, London, p 435

    Google Scholar 

  • Dangé AD (1986) Changes in carbohydrates metabolism in Tilapia, Oreochromis (Sarotherodon) mossambicus, during short-term exposure to different type of pollutants. Environ Pollut 41A:165–177

    Google Scholar 

  • Datta S, Saha DR, Gosh D, Majumdar T, Bhattacharya S, Mazumder S (2007) Sub-lethal concentration of arsenic interferes with the proliferation of hepatocytes and induces in vivo apoptosis in Clarias batrachus L. Comp Biochem Physiol 145:339–349

    Google Scholar 

  • De Boeck G, Nago TT, Van Campenhout K, Blust R (2003) Differential mettalothionein induction pattern in three freshwater fish during sublethal copper exposure. Aquat Toxicol 65:413–424

    Article  PubMed  Google Scholar 

  • Dumas BT, Biggs HG (1972) In: Standard methods of clinical chemistry, vol 7. Academic Press, New York, USA, pp 175

  • Eisler R (1998) Copper hazards to fish, wildlife, and invertebrates: a synoptic review. US geological survey, biological resources division, biological science report USGS/BRD/BSR-1997–0002. Containment hazard reviews report, vol 33, pp 98

  • Environmental Protection Agency (1993) Methods for measuring the acute toxicity of effluents and receiving waters to freshwater and marine organisms, 4th edn. US Environmental Protection Agency. EPA/600/4-90/027F

  • Flemming CA, Trevors JT (1989) Copper toxicity and chemistry in the environment: a review. Water Air Soil Poll 44:143–158

    Article  CAS  Google Scholar 

  • Foss A, Imsland A, Vikingstad E, Stefansson S, Norberg B, Pedersen S, Sandvik T, Roth B (2009) Compensatory growth in Atlantic halibut: effect of starvation and subsequent feeding on growth, maturation, feed utilization and flesh quality. Aquaculture 290:304–310

    Article  Google Scholar 

  • Gill TS, Epple A (1993) Stress-related changes in the hematological profile of the American eel, Anguilla rostrata. Ecotoxicol Environ Safe 25:227–235

    Article  CAS  Google Scholar 

  • Goodyear KI, McNeill S (1999) Bioaccumulation of heavy metals by aquatic macro-invertebrates of different feeding guilds: a review. Sci Total Environ 229(1–2):1–19

    CAS  Google Scholar 

  • Gravato C, Teles M, Oliveira M, Santos MA (2006) Oxidative stress, liver biotransformation and genotoxic effects induced by copper in Anguilla anguilla L.—the influence of pre-exposure to β-naphthoflavone. Chemosphere 65(10):1821–1830

    Article  PubMed  CAS  Google Scholar 

  • Handy RD, Sims DW, Giles A, Campbell HA, Musonda MM (1999) Metabolic trade-off between locomotion and detoxification for maintenance of blood chemistry and growth parameters by rainbow trout (Onchorhynchus mykiss) during chronic dietary exposure to copper. Aquat Toxicol 47:23–41

    Article  CAS  Google Scholar 

  • Hashemi S, Blust R, De Boeck G (2007) The effect of food rations on the tissue specific copper accumulation patterns of sublethal waterborne exposure in Cyprinus carpio. Environ Toxicol Chem 26(7):1507–1511

    Article  PubMed  CAS  Google Scholar 

  • Hashemi S, Kunwar P, Blust R, Boeck GD (2008a) Differential metallothionein induction patterns in fed and starved carp (Cyprinus carpio) during the water borne copper exposure. Environ Toxicol Chem 27:2154–2158

    Article  PubMed  CAS  Google Scholar 

  • Hashemi S, Blust R, Boeck GD (2008b) The effect of starving and feeding on copper toxicity and uptake in Cu acclimated and non-acclimated carp. Aquat Toxicol 86:142–147

    Article  PubMed  CAS  Google Scholar 

  • Henry RJ (1964) Clinical chemistry (principles and techniques). Harper & Row, New York, pp 181–747

    Google Scholar 

  • Hori TSF, Avilez IM, Inoue LK, Moraes G (2006) Metabolical changes induced by chronic phenol exposure in matrinxã Brycon cephalus I (teleostei: characidae) juveniles. Comp Biochem Physiol C 143(1):67–72

    Article  Google Scholar 

  • Hoyle I, Shaw BJ, Handy RD (2007) Dietary exposure in African walking catfish, Clarias gariepinus: transient osmoregulatory disturbances and oxidative stress. Aquat Toxicol 83:62–72

    Article  PubMed  CAS  Google Scholar 

  • Kunwar PS, Taudorache C, Ecykmans M, Bulst R, De Boek G (2009) Influence of food ration, copper exposure and exercise on energy metabolism of common carp (Cyprinus carpio). Comp Biochem Physiol C 149(1):113–119

    Google Scholar 

  • Laflamme JS, Couillard Y, Campbell PGC, Hontela A (2000) Interrenal metallothionein and cortisol secretion in relation to Cd, Cu and Zn exposure in yellow perch, Perca flavescens Abitibi lakes. Can J Fish Aquat Sci 57:1692–1700

    Article  CAS  Google Scholar 

  • Larsen BK, Pörtner H-O, Jensen FB (1997) Extra-and intracellular acid-base balance and ionic regulation in cod (Gadus morhua) during combined and isolated exposures to hypercapnia and copper. Mar Biol 128:237–346

    Article  Google Scholar 

  • Lee RG, Foerster J, Jukens J, Paraskevas F, Greer JP, Rodgers GM (1998) Wintrobe’s—clinical hematology, 10th edn. Lippincott Williams & Wilkins, New York

    Google Scholar 

  • Levesque HM, Moon TW, Campbell PGC, Hontela A (2002) Seasonal variation in carbohydrate and lipid metabolism of yellow perch (Perca flavescens) chronically exposed to metals in the field. Aquat Toxicol 60:257–267

    Article  PubMed  CAS  Google Scholar 

  • Lushchank VI, Bagnyukova TV (2006a) Temperature increase results in oxidative stress in goldfish tissues: 1. Indices of oxidative stress. Comp Biochem Physiol C 143:30–35

    Google Scholar 

  • Lushchank VI, Bagnyukova TV (2006b) Temperature increase results in oxidative stress in goldfish tissues: 2. Antioxidant and associated enzymes. Comp Biochem Physiol C 143:36–41

    Google Scholar 

  • McGeer JC, Szebedinszky C, McDonald DG, Wood CM (2002) The role of dissolved organic carbon in moderating the bioavailability and toxicity of Cu to rainbow trout during chronic waterborne exposure. Comp Biochem Physiol C 133:147–160

    Google Scholar 

  • Nawaz M, Manzl C, Lacher V, Krumschnabel G (2006) Copper induced stimulation of extracellular signal-regulated kinase in trout hepatocytes: the role of reactive oxygen species, Ca2+, and cell energetic and the impact of extracellular signal-regulated kinase signaling on apoptosis and necrosis. Toxicol Sci 92:464–475

    Article  PubMed  CAS  Google Scholar 

  • Oliveira M, Serafim M, Bebianno MJ, Pacheco M, Santos MA (2008) European eel (Anguilla Anguilla L.) metallothionein, endocrine, metabolic and genotoxic responses to copper exposure. Ecotoxicol Environ Safe 70:20–26

    Article  CAS  Google Scholar 

  • Olsen RE, Sundell K, RingØ E, Myklebust R, Hemre G (2008) The acute stress response in fed and food deprived Atalntic cod, Gadus morhua L. Aquaculture 280:232–241

    Article  Google Scholar 

  • Oser BL (1979) Hawks physiological chemistry, blakisten division. Mc Graw-Hill, New York, pp 783–784

    Google Scholar 

  • Pait AS, Nelson JO (2003) Vitellogenesis in male Fundulus heteroclitus (Killifish) induced by selected estrogenic compounds. Aquat Toxicol 64:331–342

    Article  PubMed  CAS  Google Scholar 

  • Papagiannis I, Kagalou I, Leonardos J, Petridis D, Kalfakakou V (2004) Copper and zinc in four freshwater fish species from Lake Pamvotis (Greece). Environ Internat 30(3):357–362

    Article  CAS  Google Scholar 

  • Pincus MR (1996) Interpreting laboratory results: reference values and decision making. In: Henry JB (ed) Clinical diagnosis and management by laboratory methods, 19th edn. W. B. Saunders, Philadelphia, pp 74–91

    Google Scholar 

  • Pipkin FB (1984) Medical statistics made easy. Churchill Livingstone, Edinburgh, p 137

    Google Scholar 

  • Ramos-Vasconcelos GR, Cardoso LA, Hermes-Lima M (2005) Seasonal modulations of free radical metabolism in estivating land snails Helix aspersa. Comp Biochem Physiol C 140:165–174

    Article  Google Scholar 

  • Řehulka J, Minařik B, Řehulkovà E (2004) Red blood cell indices of rainbow trout, Oncorhynchus mykiss (Walbaum) in aquaculture. Aquac Res 35:529–546

    Article  Google Scholar 

  • Reitman S, Frankel AS (1957) A colorimetric method for the determination of serum glutamic oxaloacetic and glutamic pyruvic transaminase. Am J Clin Pathol 28:56–63

    PubMed  CAS  Google Scholar 

  • Ribas L, Flos R, Reig L, MacKenzie S, Barton BA, Tort L (2007) Comparison of methods for anaesthetizing Senegal sole (Solea senegalenesis) before slaughter: stress responses and final product quality. Aquaculture 269(1–4):250–258

    Article  CAS  Google Scholar 

  • Roy S, Bhattacharya S (2006) Arsenic-induced histopathology and synthesis of stress proteins in liver of Channa punctatus. Ecotoxicol Eniviron Saf 65:218–229

    Article  CAS  Google Scholar 

  • Sanchez W, Ait-Aissa S, Palluel O, Ditche JM, Porcher JM (2007) Preliminary investigation of multi-biomarker response in three-spined stickleback (Gasterosteus aculeatus L.) sample in contaminated streams. Ecotoxicology 16:279–287

    Article  PubMed  CAS  Google Scholar 

  • Sanchez W, Piccini B, Ditche J, Porcher J (2008) Assessment of seasonal variability of biomarkers in three-spined stickleback (Gasterossteus aculeatus L.) form a low contaminated stream: implication for environmental biomonitoring. Environ Internat 34:791–798

    Article  Google Scholar 

  • Shah SL (2006) Hematological parameters in tench Tinca tinca after short term exposure to lead. J Appl Toxicol 26:223–228

    Article  PubMed  CAS  Google Scholar 

  • Shah SL, Altinndag A (2004) Hematological parameters of tench (Tinca tinca L., 1758) on acute and chronic exposures of lethal and sublethal treatments of cadmium. Fresen Environ Bull 13:1477–1481

    CAS  Google Scholar 

  • Sharaf-Eldeen K, Abdel-Hameid N (2002) Sublethal effects of copper sulphate, malathion and paraquat on protein pattern of Oreochromis niloticus. Egypt J Aquat Biol Fish 6(2):167–182

    Google Scholar 

  • Tort L, Torres P, Flos R (1987) Effects on dogfish haematology and liver composition after acute copper exposure. Comp Biochem Physiol C87(2):349–353

    Google Scholar 

  • Trinder P (1969) Determination of glucose in blood using glucose oxidase with an alternative oxygen acceptor. Annal Clin Biochem 6:24–27

    CAS  Google Scholar 

  • Uriu-Adams JY, Kleen CL (2005) Copper, oxidative stress, and human health. Mol Aspects Med 26:268–298

    Article  PubMed  CAS  Google Scholar 

  • Van de Nieuwegiessen PG, Olwo J, Khong S, Verreth JAJ, Schrama JW (2009) Effects of age and stocking density on the welfare of African catfish, Clarias gariepinus Burchell. Aquaculture 288:69–75

    Article  Google Scholar 

  • Van der Oost R, Beyer J, Vermeulen NPE (2003) Fish bioaccumulation and biomarkers in environmental risk assessment: a review. Environ Toxicol Pharmacol 13:57–149

    Article  PubMed  Google Scholar 

  • Webener V, Van Vuren JHJ, Du Preez HH (1992) Effect of manganese and iron at neutral and acidic pH on the hematology of banded tilapia (Tilapia sparrmanii). Bull Environ Contam Toxicol 49:613–619

    Google Scholar 

  • WHO (1993) The control of schistosomiasis: second report of the WHO expert committee, WHO technical report series 830, WHO Geneva

  • WHO (1998) Environmental health criteria 200. In: Copper. IPCS-International programme on chemical safety, WHO, Geneva

  • Yılmaz AB, Sangün MK, Yağlioğlu D, Turan C (2010) Metals (major, essential to non-essential) composition of the different tissues of three demersal fish species from İskenderun Bay, Turkey. Food Chemistry doi:10.1016/j.foodchem.2010.04.057

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Nassr-Allah H. Abdel-Hameid.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Abdel-Hameid, NA.H. Effect of starving and feeding on some haematological and physiological responses of the Nile catfish, Clarias gariepinus exposed to copper at extreme seasons. Fish Physiol Biochem 37, 875–884 (2011). https://doi.org/10.1007/s10695-011-9485-0

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s10695-011-9485-0

Keywords